Aušra Matulevičienė

498 citations

24 papers · 348 indexed · h-index 10

Co-authors: Vaidutis Kučinskas Laima Ambrozaitytė Algirdas Utkus Mare Saag Triin Jagomägi Andres Metspalu Tiit Nikopensius Thomy de Ravel
Topics: Genomic variations and chromosomal abnormalities (6 papers)Cleft Lip and Palate Research (6 papers)Craniofacial Disorders and Treatments (4 papers)
Cited by: Genetics Ophthalmology
Journals: SHILAP Revista de lepidopterologíaThe Journal of Clinical Endocrinology & Metabolism Medicine
Partner nations: Lithuania Latvia Estonia

In The Last Decade

Aušra Matulevičienė

23 papers receiving 344 citations

Peers

Countries citing papers authored by Aušra Matulevičienė

Since Specialization

Citations

This map shows the geographic impact of Aušra Matulevičienė's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Aušra Matulevičienė with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aušra Matulevičienė more than expected).

Fields of papers citing papers by Aušra Matulevičienė

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aušra Matulevičienė. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Aušra Matulevičienė. The network helps show where Aušra Matulevičienė may publish in the future.

Co-authorship network of co-authors of Aušra Matulevičienė

This figure shows the co-authorship network connecting the top 25 collaborators of Aušra Matulevičienė. A scholar is included among the top collaborators of Aušra Matulevičienė based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aušra Matulevičienė. Aušra Matulevičienė is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Neuropsychiatric Aspects of Sotos Syndrome: Explorative Review Building Multidisciplinary Bridges in Clinical Practice 2024 ·Journal of Clinical Medicine ·Sigita Lesinskienė,(unknown),(unknown),Aušra Matulevičienė,Algirdas Utkus	3
2	Psychological distress 35 years after the Chornobyl accident in the Lithuanian clean-up workers 2023 ·Global Health Action ·Evaldas Kazlauskas,Giedrė Smailytė,(unknown),Vaidutis Kučinskas,Aušra Matulevičienė,Ask Elklit,(unknown),Laima Ambrozaitytė	0
3	Consensus recommendations on chewing, swallowing and gastrointestinal problems in Phelan-McDermid syndrome 2023 ·European Journal of Medical Genetics ·Aušra Matulevičienė,(unknown),Els Kuiper,Andreas M. Grabrucker	10
4	Significant Association Between Huntingtin Gene Mutation and Prevalence of Hopelessness, Depression and Anxiety Symptoms 2021 ·SHILAP Revista de lepidopterología ·(unknown),Robertas Strumila,Aistė Lengvenytė,(unknown),(unknown),Aušra Matulevičienė,(unknown),Algirdas Utkus	2
5	A novel variant in the PDE4D gene is the cause of Acrodysostosis type 2 in a Lithuanian patient: a case report 2021 ·BMC Endocrine Disorders ·(unknown),(unknown),(unknown),Loreta Cimbalistienė,(unknown),Aušra Matulevičienė,Algirdas Utkus,Eglė Preikšaitienė	1
6	Juvenile Huntington’s disease: two case reports and a review of the literature 2020 ·Journal of Medical Case Reports ·Sigita Lesinskienė,(unknown),Rūta Praninskienė,(unknown),Aušra Matulevičienė,Algirdas Utkus	7
7	HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence 2020 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown),Robert Meyer,(unknown),Laima Ambrozaitytė,Aušra Matulevičienė,Florian Kraft,Matthias Begemann,Miriam Elbracht,Thomas Eggermann	13
8	Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies 2017 ·Medicine ·(unknown),(unknown),Aušra Matulevičienė,Birutė Burnytė,(unknown),Laima Ambrozaitytė,(unknown),(unknown),Algirdas Utkus,Vaidutis Kučinskas	5
9	The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population 2016 ·BMC Genetics ·(unknown),Audronė Jakaitienė,(unknown),(unknown),Eglė Preikšaitienė,Birutė Burnytė,Biruté Tumiene,Aušra Matulevičienė,Laima Ambrozaitytė,Ingrida Uktverytė,(unknown),(unknown),Loreta Cimbalistienė,Eugenijus Lesinskas,Vaidutis Kučinskas,Algirdas Utkus	18
10	Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies 2016 ·BMC Musculoskeletal Disorders ·Inna Inashkina,Eriks Jankevics,(unknown),(unknown),(unknown),Ieva Mičule,Jurģis Strautmanis,(unknown),Loreta Cimbalistienė,Vaidutis Kučinskas,Astrīda Krūmiņa,Algirdas Utkus,Birutė Burnytė,Aušra Matulevičienė,Baiba Lāce	8
11	NSD1 duplication in Silver–Russell syndrome (SRS): molecular karyotyping in patients with SRS features 2016 ·Clinical Genetics ·(unknown),Robert Meyer,G. Fekete,Stephanie Spranger,Aušra Matulevičienė,Vaidutis Kučinskas,(unknown),Andrea Luczay,Nadina Ortiz Brüchle,Katja Eggermann,Klaus Zerres,Miriam Elbracht,Thomas Eggermann	20
12	Frame shift mutations of the ZMPSTE24 gene in two siblings with restrictive dermopathy 2015 ·Clinical Dysmorphology ·Aušra Matulevičienė,(unknown),(unknown),Laima Ambrozaitytė,Raimundas Meškauskas,(unknown),(unknown),Algirdas Utkus,Vaidutis Kučinskas	5
13	Association of BMP4 polymorphisms with non-syndromic cleft lip with or without cleft palate and isolated cleft palate in Latvian and Lithuanian populations. 2014 ·PubMed ·(unknown),Laima Ambrozaitytė,(unknown),Ilze Akota,(unknown),Astrīda Krūmiņa,Aušra Matulevičienė,Algirdas Utkus,(unknown),Baiba Lāce	10
14	Familial Distal Monosomy 5p15.3-pter With Trisomy 12q24.2-qter Resulting in Neurodevelopmental Delay and Dysmorphic Features 2013 ·Journal of Child Neurology ·(unknown),Aušra Matulevičienė,(unknown),(unknown),Jūratė Kasnauskienė,Vaidutis Kučinskas	1
15	A single gene deletion on 4q28.3: PCDH18 – A new candidate gene for intellectual disability? 2012 ·European Journal of Medical Genetics ·Jūratė Kasnauskienė,(unknown),Eglė Preikšaitienė,Aušra Matulevičienė,(unknown),George Koumbaris,Carolina Sismani,(unknown),Philippos C. Patsalis,Vaidutis Kučinskas	15
16	Variation in FGF1, FOXE1, and TIMP2genes is associated with nonsyndromic cleft lip with or without cleft palate 2011 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Tiit Nikopensius,(unknown),Laima Ambrozaitytė,Triin Jagomägi,Mare Saag,Aušra Matulevičienė,Algirdas Utkus,Kaarel Krjutškov,(unknown),Linda Gailīte,Ilze Akota,(unknown),Astrīda Krūmiņa,Jānis Kloviņš,Baiba Lāce,Vaidutis Kučinskas,Andres Metspalu	38
17	Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes 2010 ·Human Mutation ·Frauke Coppieters,Ingele Casteels,Françoise Meire,Sarah De Jaegere,(unknown),Nicole Van Regemorter,Hilde Van Esch,Aušra Matulevičienė,Luís Nunes,(unknown),Sophie Walraedt,(unknown),Paul Coucke,(unknown),Hester Y. Kroes,Johan Vande Walle,Thomy de Ravel,Bart P. Leroy,Elfride De Baere	110
18	Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate 2010 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Tiit Nikopensius,Triin Jagomägi,Kaarel Krjutškov,(unknown),Mare Saag,(unknown),Linda Gailīte,Ilze Akota,(unknown),Astrīda Krūmiņa,Laima Ambrozaitytė,Aušra Matulevičienė,Zita Aušrelė Kučinskienė,Baiba Lāce,Vaidutis Kučinskas,Andres Metspalu	37
19	Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients 2009 ·American Journal of Medical Genetics Part A ·Tiit Nikopensius,Laima Ambrozaitytė,Kerstin U. Ludwig,Stefanie Birnbaum,Triin Jagomägi,Mare Saag,Aušra Matulevičienė,Laura Linkevičienė,Stefan Herms,Michael Knapp,Per Hoffmann,Markus M. Nöthen,Vaidutis Kučinskas,Andres Metspalu,Elisabeth Mangold	30
20	Orofacial clefts with associated anomalies in Lithuania 2007 ·Acta medica Lituanica ·(unknown),Aušra Matulevičienė,Algirdas Utkus,Vaidutis Kučinskas,Laura Linkevičienė	2

About Aušra Matulevičienė

Aušra Matulevičienė is a scholar working on Genetics, Sensory Systems and Biological Psychiatry, having authored 24 papers that have together received 348 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Cleft Lip and Palate Research (6 papers) and Craniofacial Disorders and Treatments (4 papers). The work is most often cited by research in Genetics (216 citations), Ophthalmology (61 citations) and Genetics (38 citations). Aušra Matulevičienė has collaborated with scholars based in Lithuania, Latvia and Estonia. Frequent co-authors include Vaidutis Kučinskas, Laima Ambrozaitytė, Algirdas Utkus, Mare Saag, Triin Jagomägi, Andres Metspalu, Tiit Nikopensius, Thomy de Ravel, Ilze Akota and Baiba Lāce. Their work appears in journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Medicine.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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